Canonical Allele Identifier: CA503596737
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2771888
ClinVar RCV Id: RCV003517837
dbSNP Id: rs1568104775
MyVariant Identifiers: chr18:g.29099795G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31519832G>T , CM000680.2:g.31519832G>T GRCh38
NC_000018.9:g.29099795G>T , CM000680.1:g.29099795G>T GRCh37
NC_000018.8:g.27353793G>T NCBI36
NG_007072.3:g.26591G>T , LRG_397:g.26591G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682241.2:c.111G>T ENSP00000507600.2:p.Leu37=
ENST00000683654.1:c.111G>T ENSP00000506971.1:p.Leu37=
ENST00000261590.13:c.111G>T MANE Select ENSP00000261590.8:p.Leu37=
ENST00000261590.12:c.111G>T ENSP00000261590.8:p.Leu37=
ENST00000585206.1:c.111G>T ENSP00000462503.1:p.Leu37=
NM_001943.3:c.111G>T , LRG_397t1:c.111G>T NP_001934.2:p.Leu37=
NM_001943.4:c.111G>T NP_001934.2:p.Leu37=
XM_024451095.1:c.-424G>T XP_024306863.1:n.-424G>T
NM_001943.5:c.111G>T MANE Select NP_001934.2:p.Leu37=